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Annane D, Sébille V, Charpentier C, et al. Effect of Treatment With Low Doses of Hydrocortisone and Fludrocortisone on Mortality in Patients With Septic Shock. JAMA. 2002;288(7):862–871. doi:10.1001/jama.288.7.862
Author Affiliations: Service de Réanimation Médicale, Hôpital Raymond Poincaré, Université de Paris V, Faculté de Médecine Paris-Ouest, Garches (Dr Annane); Service de Pharmacologie, Unité de Pharmacologie Clinique, Hôpital de Pontchaillou, Université de Rennes I, Rennes (Drs Sébille and Bellissant); Service de Réanimation Chirurgicale (Dr Charpentier) and de Réanimation Médicale (Dr Bollaert), Hôpital Central, Nancy; the Service de Réanimation Polyvalente, Hôpital Dupuytren, Limoges (Dr François); Service de Réanimation Polyvalente, Centre Hospitalier, Chalons en Champagne (Dr Korach); Service de Réanimation Médicale, Hôpital Jean Minjoz, Besançon (Dr Capellier); Service de Réanimation Médico-Chirurgicale, Hôpital Avicenne, Bobigny (Dr Cohen); Service de Réanimation Médicale (Dr Azoulay) and Délégation à la Recherche Clinique, Assistance Publique-Hôpitaux de Paris (Dr Chaumet-Riffaut), Hôpital Saint-Louis, Paris; and the Service de Réanimation Chirurgicale, Hôpital Antoine Béclère, Clamart (Dr Troché), France. Dr Sébille is now at the Loboratoire de Biostatistiques at the Faculté de Pharmacie at the Université de Nantes, France.
Caring for the Critically Ill Patient Section Editor: Deborah J. Cook, MD, Consulting Editor, JAMA.
Context Septic shock may be associated with relative adrenal insufficiency.
Thus, a replacement therapy of low doses of corticosteroids has been proposed
to treat septic shock.
Objective To assess whether low doses of corticosteroids improve 28-day survival
in patients with septic shock and relative adrenal insufficiency.
Design and Setting Placebo-controlled, randomized, double-blind, parallel-group trial performed
in 19 intensive care units in France from October 9, 1995, to February 23,
Patients Three hundred adult patients who fulfilled usual criteria for septic
shock were enrolled after undergoing a short corticotropin test.
Intervention Patients were randomly assigned to receive either hydrocortisone (50-mg
intravenous bolus every 6 hours) and fludrocortisone (50-µg tablet once
daily) (n = 151) or matching placebos (n = 149) for 7 days.
Main Outcome Measure Twenty-eight-day survival distribution in patients with relative adrenal
insufficiency (nonresponders to the corticotropin test).
Results One patient from the corticosteroid group was excluded from analyses
because of consent withdrawal. There were 229 nonresponders to the corticotropin
test (placebo, 115; corticosteroids, 114) and 70 responders to the corticotropin
test (placebo, 34; corticosteroids, 36). In nonresponders, there were 73 deaths
(63%) in the placebo group and 60 deaths (53%) in the corticosteroid group
(hazard ratio, 0.67; 95% confidence interval, 0.47-0.95; P = .02). Vasopressor therapy was withdrawn within 28 days in 46 patients
(40%) in the placebo group and in 65 patients (57%) in the corticosteroid
group (hazard ratio, 1.91; 95% confidence interval, 1.29-2.84; P = .001). There was no significant difference between groups in responders.
Adverse events rates were similar in the 2 groups.
Conclusion In our trial, a 7-day treatment with low doses of hydrocortisone and
fludrocortisone significantly reduced the risk of death in patients with septic
shock and relative adrenal insufficiency without increasing adverse events.
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